Semi-automated solid phase extraction method for the mass spectrometric quantification of 12 specific metabolites of organophosphorus pesticides, synthetic pyrethroids, and select herbicides in human urine

•Developed and validated a method for the measurement of these analytes in urine.•The method is highly efficient using automation for preparation and analysis.•High mass resolution analysis reduces chemical noise and increases sensitivity.•Smaller diameter, smaller pore size chromatography column im...

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Veröffentlicht in:Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2013-06, Vol.929, p.18-26
Hauptverfasser: Davis, Mark D., Wade, Erin L., Restrepo, Paula R., Roman-Esteva, William, Bravo, Roberto, Kuklenyik, Peter, Calafat, Antonia M.
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Sprache:eng
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Zusammenfassung:•Developed and validated a method for the measurement of these analytes in urine.•The method is highly efficient using automation for preparation and analysis.•High mass resolution analysis reduces chemical noise and increases sensitivity.•Smaller diameter, smaller pore size chromatography column improves chromatography. Organophosphate and pyrethroid insecticides and phenoxyacetic acid herbicides represent important classes of pesticides applied in commercial and residential settings. Interest in assessing the extent of human exposure to these pesticides exists because of their widespread use and their potential adverse health effects. An analytical method for measuring 12 biomarkers of several of these pesticides in urine has been developed. The target analytes were extracted from one milliliter of urine by a semi-automated solid phase extraction technique, separated from each other and from other urinary biomolecules by reversed-phase high performance liquid chromatography, and detected using tandem mass spectrometry with isotope dilution quantitation. This method can be used to measure all the target analytes in one injection with similar repeatability and detection limits of previous methods which required more than one injection. Each step of the procedure was optimized to produce a robust, reproducible, accurate, precise and efficient method. The required selectivity and sensitivity for trace-level analysis (e.g., limits of detection below 0.5ng/mL) was achieved using a narrow diameter analytical column, higher than unit mass resolution for certain analytes, and stable isotope labeled internal standards. The method was applied to the analysis of 55 samples collected from adult anonymous donors with no known exposure to the target pesticides. This efficient and cost-effective method is adequate to handle the large number of samples required for national biomonitoring surveys.
ISSN:1570-0232
1873-376X
DOI:10.1016/j.jchromb.2013.04.005